Lead complex, multi-product initiatives that deliver innovative medical devices to market. Inspire cross-functional teams, drive program success, and ensure compliance with ISO and FDA regulations.
Requirements
- 8+ years of experience leading new product development programs in regulated industries, preferably medical devices
- Experience with acquisition integration teams and global product launches
- Strong familiarity with New Product Introduction (NPI) methodologies, medical device design cycles, and industry standards
- In-depth understanding of ISO and FDA regulations, including design control procedures
- Expertise in risk management and dependency mitigation throughout program lifecycles
- Proficiency in project management tools such as Smartsheet, Planview, Microsoft Project, and dashboards
- Exceptional leadership, communication, and influence management skills to foster collaboration across matrix organizations
- Proven ability to manage multiple large-scale projects simultaneously in varying lifecycle stages
- Master’s Degree preferred (technical or non-technical); PhD is a plus
- PMP certification is beneficial but not required
Benefits
- Competitive salary
- Annual bonus scheme
- Comprehensive training and development opportunities
- Continued development and training throughout career